A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916750



Internal ID22691969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64818740..64823337hg38UCSC Ensembl
chr11:64586212..64590809hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384598
hg194598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv268n209
Supporting Variantsnssv17357166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916750
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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